RUNX1T1 is overexpressed in imatinib mesylate-resistant cells

被引:6
作者
Binato, Renata [1 ]
Mencalha, Andre [1 ]
Pizzatti, Luciana [1 ]
Scholl, Vanessa [1 ]
Zalcberg, Ilana [1 ]
Abdelhay, Eliana [1 ]
机构
[1] INCa, Div Labs CEMO, Ctr Transplante Medula Ossea, BR-20230130 Rio De Janeiro, Brazil
关键词
RUNX1T1; BCR-ABL; imatinib mesylate; chip array; overexpressed genes; resistant cell lines; MYELOGENOUS LEUKEMIA-CELLS; CHRONIC MYELOID-LEUKEMIA; BCR-ABL INDEPENDENCE; EXPRESSION; MECHANISMS; PROTEIN; IDENTIFICATION; SENSITIVITY; INHIBITION; LINE;
D O I
10.3892/mmr_00000153
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The Philadelphia (Ph) chromosome, which occurs as a result of a translocation between chromosomes 9 and 22, generates a BCR-ABL fusion oncogene in leukaemia cells. The BCR-ABL fusion protein has constitutive tyrosine kinase activity. The development of imatinib mesylate (ST1571, Gleevec (R)), a potent and selective BCR-ABL tyrosine kinase inhibitor, represents an important advance in cancer therapy. However, inherent mechanisms confer resistance to imatinib mesylate in some leukaemia patients. In order to identify the genes potentially related to these resistance mechanisms, we examined genes differentially expressed in BCR-ABL-positive cell lines resistant to imatinib mesylate. A comparison of global gene expression using the HG-U133 2.0 plus Gene Chip array was first performed. Twenty-three genes were shown to be overexpressed in an imatinib-resistant cell line. Among these, RUNX1T1 was shown to be overexpressed in another resistant cell line and in patients resistant to imatinib mesylate. This Suggests that RUNX1T1 is a putative candidate for the further study of imatinib mesylate resistance.
引用
收藏
页码:657 / 661
页数:5
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